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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189756Generated: October 25, 2026

1-Isopropylpiperazine → 2-(4-Isopropyl-piperazin-1-yl)-5-nitro-pyrimidine

https://huagongshe.com/reaction/1189756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IsopropylpiperazineHCID 78013—
Reactant2-Chloro-5-nitropyrimidineHCID 82544—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(4-Isopropyl-piperazin-1-yl)-5-nitro-pyrimidineHCID 6691466789.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

1-Isopropylpiperazine (1.8 mL, 12.7 mmol, 2 equiv) was added to a cold (5° C.) solution of 2-chloro-5-nitropyrimidine (1 g, 6.3 mmol,) in DCM (5 mL). The reaction mixture was stirred for 20 min at 5° C. and then diluted with DCM and H2O. The aqueous layer was separated and extracted with DCM. The organic phase was washed with brine, dried (Na2SO4), filtered and concentrated to provide 1.41 g of the title compound as a beige solid: ESI-MS: 252.2 [M+H]+; tR=1.89 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674099B2
Source datasetuspto-grants-2014_03
ORD IDord-c38b6be6353e41d3b81cdc6b0c5888b2
Source noteuspto-grants-2014_03